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Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity
BACKGROUND: Glioblastoma is the most common and most lethal form of brain tumor in human. Unfortunately, there is still no effective therapy to this fatal disease and the median survival is generally less than one year from the time of diagnosis. Discovery of ligands that can bind specifically to th...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462804/ https://www.ncbi.nlm.nih.gov/pubmed/23056171 http://dx.doi.org/10.1371/journal.pone.0042731 |
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author | Kang, Dezhi Wang, Jiangjie Zhang, Weiyun Song, Yanling Li, Xilan Zou, Yuan Zhu, Mingtao Zhu, Zhi Chen, Fuyong Yang, Chaoyong James |
author_facet | Kang, Dezhi Wang, Jiangjie Zhang, Weiyun Song, Yanling Li, Xilan Zou, Yuan Zhu, Mingtao Zhu, Zhi Chen, Fuyong Yang, Chaoyong James |
author_sort | Kang, Dezhi |
collection | PubMed |
description | BACKGROUND: Glioblastoma is the most common and most lethal form of brain tumor in human. Unfortunately, there is still no effective therapy to this fatal disease and the median survival is generally less than one year from the time of diagnosis. Discovery of ligands that can bind specifically to this type of tumor cells will be of great significance to develop early molecular imaging, targeted delivery and guided surgery methods to battle this type of brain tumor. METHODOLOGY/PRINCIPAL FINDINGS: We discovered two target-specific aptamers named GBM128 and GBM131 against cultured human glioblastoma cell line U118-MG after 30 rounds selection by a method called cell-based Systematic Evolution of Ligands by EXponential enrichment (cell-SELEX). These two aptamers have high affinity and specificity against target glioblastoma cells. They neither recognize normal astraglial cells, nor do they recognize other normal and cancer cell lines tested. Clinical tissues were also tested and the results showed that these two aptamers can bind to different clinical glioma tissues but not normal brain tissues. More importantly, binding affinity and selectivity of these two aptamers were retained in complicated biological environment. CONCLUSION/SIGNIFICANCE: The selected aptamers could be used to identify specific glioblastoma biomarkers. Methods of molecular imaging, targeted drug delivery, ligand guided surgery can be further developed based on these ligands for early detection, targeted therapy, and guided surgery of glioblastoma leading to effective treatment of glioblastoma. |
format | Online Article Text |
id | pubmed-3462804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34628042012-10-10 Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity Kang, Dezhi Wang, Jiangjie Zhang, Weiyun Song, Yanling Li, Xilan Zou, Yuan Zhu, Mingtao Zhu, Zhi Chen, Fuyong Yang, Chaoyong James PLoS One Research Article BACKGROUND: Glioblastoma is the most common and most lethal form of brain tumor in human. Unfortunately, there is still no effective therapy to this fatal disease and the median survival is generally less than one year from the time of diagnosis. Discovery of ligands that can bind specifically to this type of tumor cells will be of great significance to develop early molecular imaging, targeted delivery and guided surgery methods to battle this type of brain tumor. METHODOLOGY/PRINCIPAL FINDINGS: We discovered two target-specific aptamers named GBM128 and GBM131 against cultured human glioblastoma cell line U118-MG after 30 rounds selection by a method called cell-based Systematic Evolution of Ligands by EXponential enrichment (cell-SELEX). These two aptamers have high affinity and specificity against target glioblastoma cells. They neither recognize normal astraglial cells, nor do they recognize other normal and cancer cell lines tested. Clinical tissues were also tested and the results showed that these two aptamers can bind to different clinical glioma tissues but not normal brain tissues. More importantly, binding affinity and selectivity of these two aptamers were retained in complicated biological environment. CONCLUSION/SIGNIFICANCE: The selected aptamers could be used to identify specific glioblastoma biomarkers. Methods of molecular imaging, targeted drug delivery, ligand guided surgery can be further developed based on these ligands for early detection, targeted therapy, and guided surgery of glioblastoma leading to effective treatment of glioblastoma. Public Library of Science 2012-10-02 /pmc/articles/PMC3462804/ /pubmed/23056171 http://dx.doi.org/10.1371/journal.pone.0042731 Text en © 2012 Kang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kang, Dezhi Wang, Jiangjie Zhang, Weiyun Song, Yanling Li, Xilan Zou, Yuan Zhu, Mingtao Zhu, Zhi Chen, Fuyong Yang, Chaoyong James Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity |
title | Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity |
title_full | Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity |
title_fullStr | Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity |
title_full_unstemmed | Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity |
title_short | Selection of DNA Aptamers against Glioblastoma Cells with High Affinity and Specificity |
title_sort | selection of dna aptamers against glioblastoma cells with high affinity and specificity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462804/ https://www.ncbi.nlm.nih.gov/pubmed/23056171 http://dx.doi.org/10.1371/journal.pone.0042731 |
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